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TCTAP 2026

Left Main Revascularization Hinges on Individualized Choices Beyond Trial Headlines N

At TCTAP 2026, Sripal Bangalore, MD, MHA, professor of medicine at NYU Grossman School of Medicine and director of invasive and interventional cardiology at Bellevue Hospital Center, reviewed contemporary evidence comparing percutaneous coronary intervention (PCI) and coronary artery bypass grafting (CABG) for left main and multivessel coronary artery disease, framing the debate as a decision that had moved beyond a simple ¡°PCI versus surgery¡± binary. He opened with a 72-year-old woman with Canadian Cardiovascular Society (CCS) class III angina, a positive stress echocardiogram, normal ejection fraction, severe calcification of the left main, ostial LAD, and LCX, and severe Medina 1,1,1 left main bifurcation disease, underscoring that both strategies offered meaningful but different tradeoffs. No Overall Mortality Difference, but Important Subgroup Signals Drawing on a meta-analysis he co-authored (Kuno, Bangalore et al., American Heart Journal 2020) of four randomized trials—EXCEL, NOBLE, the SYNTAX left main subgroup, and PRECOMBAT (n=4,394, follow-up ¡Ã5 years)—together with the patient-level meta-analysis by Sabatine et al. (Lancet 2021;398:2247-57), Bangalore concluded that there was no overall mortality difference between PCI and CABG in left main disease. The recently reported NOBLE 10-year final results (Holck et al., Lancet 2026;407:1374-82) reinforced this finding, with all-cause mortality of 23% in the PCI arm versus 25% in the CABG arm (HR 0.93; 95% CI 0.74–1.18; p=0.56) and no significant interaction with SYNTAX score. He highlighted two clinically important subgroup signals. First, in the NOBLE acute coronary syndrome (ACS) cohort, PCI was associated with significantly lower long-term mortality than CABG (HR 0.57; 95% CI 0.32–0.99; p=0.047), suggesting that the physiology and urgency of ACS may have favored a less invasive upfront strategy in selected patients. Second, in pooled meta-analytic data, there appeared to be a possible advantage of CABG for cardiovascular death—not all-cause mortality—only at very high SYNTAX scores, indicating that anatomic complexity remained relevant for that specific endpoint at the most complex end of the spectrum. Tradeoffs Beyond Survival Bangalore explained that, across pooled trial data, CABG generally reduced spontaneous myocardial infarction and repeat revascularization, while PCI was associated with fewer peri-procedural complications, lower early stroke risk, and faster recovery. In the EXCEL quality-of-life analyses (Baron et al., JACC 2017;70:3113-22), PCI was associated with earlier improvement in physical function (SF-12 Physical Summary), dyspnea (Rose Dyspnea Scale), depression (PHQ-8), and angina frequency (Seattle Angina Questionnaire), with most differences narrowing or resolving by 12 to 36 months. His central message was that ¡°patient preference matters,¡± particularly when weighing short-term risks of death and stroke with CABG against long-term risks of repeat revascularization after PCI. Table 1. Clinical tradeoffs in PCI versus CABG decision-making Domain PCI CABG Early recovery Generally faster Longer recovery Early procedural burden Lower peri-procedural complications in selected patients Higher short-term surgical risk Repeat revascularization Higher risk Lower risk Spontaneous MI Higher than CABG in pooled datasets Lower risk Stroke / peri-procedural events Lower early burden Higher peri-procedural burden Mortality signal in subgroups Possible benefit in ACS cohort (NOBLE 10-year) Possible benefit for CV death at very high SYNTAX scores Best suited for Equivalent complete revascularization achievable, lower anatomic complexity, high surgical risk, ACS in selected patients, patient preference Complex anatomy, very high SYNTAX score, durable complete revascularization Guidelines and Patient Selection Bangalore placed his conclusions in the context of the 2021 ACC/AHA/SCAI revascularization guideline, of which he was a co-author (Lawton, Tamis-Holland, Bangalore, et al., JACC 2021). The guideline recommended CABG to improve survival in patients with significant left main stenosis (Class 1), while stating that PCI was reasonable (Class 2a) in selected stable patients for whom PCI could provide equivalent revascularization to that possible with CABG. He also cautioned that the mean age of patients enrolled in the four landmark trials had ranged from 62 to 66 years (PRECOMBAT 62; SYNTAX 65; EXCEL and NOBLE 66)—considerably younger than many patients encountered in contemporary practice. Direct extrapolation of these results to substantially older patients, including the 72-year-old in his opening case, therefore required caution. Conclusion Bangalore concluded that revascularization choice should be individualized by a Heart Team, weighing the ability to achieve complete revascularization, short- and long-term event risks, clinical presentation (including ACS status), anatomic complexity at the highest SYNTAX tier, frailty, age, and informed patient goals. TCTAP Workshops Left Main & Multi-Vessel Disease: Modern Evidence and Real-World Strategy Thursday, April 30, 2:50 PM ~ 4:25 PM Main Arena, Level 1 Watch Session Video

May 14, 2026 78

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TCTAP 2026

Antithrombotic Therapy After TAVR: Balancing Bleeding and Thrombosis N

At TCTAP 2026, Davide Capodanno, MD, PhD (University of Catania, Italy), delivered a comprehensive lecture on antithrombotic therapy after transcatheter aortic valve replacement (TAVR), focusing on how recent evidence has reshaped clinical practice and where uncertainties still remain. TAVR has rapidly expanded across all surgical risk categories, including younger and lower-risk patients. As procedural outcomes have improved, attention has increasingly shifted toward optimizing post-procedural management. Among these, antithrombotic therapy remains one of the most challenging aspects, requiring a careful balance between thrombotic risk and bleeding complications. He emphasized that contemporary management is now largely guided by the 2025 ESC/EACTS valvular heart disease guidelines. These guidelines reflect a major shift away from historically intensive antithrombotic strategies toward a simplified approach. In patients without an indication for oral anticoagulation (OAC), low-dose aspirin monotherapy was recommended as the standard treatment. This recommendation was supported by randomized trials such as POPULAR-TAVI, which demonstrated a significant reduction in bleeding without an increase in thrombotic events compared with dual antiplatelet therapy (DAPT). Accordingly, DAPT was no longer recommended in this population unless there was a clear clinical indication. The role of oral anticoagulation in patients without baseline indications was also critically reassessed. Trials such as GALILEO and ATLANTIS failed to show clinical benefit and, in some cases, suggested harm with routine anticoagulation. Based on these findings, the guidelines advised against routine use of OAC in patients undergoing TAVR without another indication. Despite these advances, several important areas of uncertainty remained. One of the most debated issues was subclinical leaflet thrombosis, typically detected as hypoattenuated leaflet thickening (HALT) on computed tomography. While HALT has been reported in a substantial proportion of patients after TAVR, its clinical significance remains unclear. Although anticoagulation has been shown to reduce imaging-detected thrombosis, this has not consistently translated into improved clinical outcomes such as stroke or mortality. He highlighted that this gap between imaging findings and clinical outcomes represents a key unresolved issue in the field. As a result, routine anticoagulation based solely on imaging findings has not been adopted in current practice. To address these uncertainties, several ongoing trials are actively investigating more refined and individualized strategies. These include CT-guided approaches, in which anticoagulation is initiated only when subclinical valve thrombosis is detected, as well as trials exploring further reduction or even discontinuation of antithrombotic therapy after TAVR. Importantly, these studies are expected to determine whether treatment decisions can be guided by imaging findings rather than applied uniformly to all patients. This represents a potential paradigm shift toward precision medicine in post-TAVR management. In patients with a clear indication for anticoagulation, such as atrial fibrillation, the strategy differed. Evidence from trials including POPULAR-TAVI and ENVISAGE-TAVI suggested that oral anticoagulation alone was generally sufficient, and that combination therapy with antiplatelet agents should be avoided whenever possible due to the increased risk of bleeding. Overall, his lecture underscored a fundamental transition in the field. Antithrombotic therapy after TAVR has evolved from empiric and intensive regimens toward a simplified, guideline-driven approach, while key clinical questions continue to be addressed through ongoing trials (Figure 1). As TAVR continues to expand into broader patient populations, the results of these studies are expected to further refine treatment strategies and shape future guidelines. Figure 1. Antithrombotic Therapy After TAVR: Simplification Amid Unanswered Questions Hot Topics TAVR Practice in 2026: Insights for the Next Era Friday, May 1, 8:30 AM ~ 9:57 AM Valve & Endovascular Theater, Level 1 Watch Session Video

May 14, 2026 59

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TCTAP 2026

Rethinking Antithrombotic Therapy in AF with Stable CAD: Are We Finally Ready to Let Go of Antiplate... N

At TCTAP 2026, Jung-Sun Kim, MD, PhD (Severance Hospital, Korea) addressed a fundamental question in current practice: whether antiplatelet therapy is still necessary in patients with atrial fibrillation (AF) and stable coronary artery disease (CAD). He noted that both the 2023 ESC and 2023 ACC/AHA guidelines recommend discontinuing antiplatelet therapy 6–12 months after percutaneous coronary intervention (PCI), with long-term management based on oral anticoagulant (OAC) monotherapy. The clinical focus, therefore, has shifted from choosing the optimal combination to determining whether any antiplatelet therapy is needed at all. To answer this question, he reviewed a series of randomized trials. The OAC-ALONE trial, although one of the earliest studies, was terminated early and failed to demonstrate non-inferiority, leaving uncertainty unresolved. The AFIRE trial provided the first major signal, showing that rivaroxaban monotherapy was superior to combination therapy for both efficacy and safety outcomes. However, its interpretation was limited by the exclusive Japanese population and use of lower-than-standard doses, raising concerns about generalizability. The EPIC-CAD trial addressed this limitation by evaluating standard-dose edoxaban in a broader population. Monotherapy significantly reduced net adverse clinical events, mainly driven by less bleeding, without increasing ischemic risk. This confirmed that direct OAC (DOAC) monotherapy can be both safe and effective at standard doses. However, the heterogeneous study population left uncertainty regarding patients with contemporary drug-eluting stents. The AQUATIC trial focused on patients with stents and high atherothrombotic risk. Even in this group, adding aspirin to OAC did not improve ischemic outcomes but increased bleeding risk, challenging the role of aspirin as the default antiplatelet agent. ¡°Clopidogrel has often shown better outcomes than aspirin for long-term antiplatelet therapy, and further evidence specifically evaluating clopidogrel-based combination therapy was needed,¡± he said. The ADAPT AF-DES trial further evaluated patients with contemporary drug-eluting stents using clopidogrel as the sole antiplatelet agent. DOAC monotherapy was non-inferior—and even superior—for net adverse clinical events, primarily due to reduced bleeding. This suggested that even clopidogrel does not provide additional benefit when combined with anticoagulation in stable patients. Clinical outcomes of the ADAPT AF DES Trial Taken together, these trials deliver a consistent message: adding antiplatelet therapy does not meaningfully reduce ischemic events but increases bleeding risk. The safety of DOAC monotherapy has been reproducible across different populations and clinical settings. ¡°Despite this, uncertainty remains in patients with high ischemic risk, such as those undergoing complex PCI or with polyvascular disease. The ongoing ADAPT AFFIRM trial is expected to provide further insight by comparing apixaban monotherapy with combination therapy in this population,¡± he said. In conclusion, he emphasized three key points. First, in patients with AF and stable CAD beyond 12 months after contemporary DES implantation, DOAC monotherapy should be considered the default strategy. Second, continued antiplatelet therapy generally increases bleeding without clear ischemic benefit. Finally, further evidence is needed in high-risk populations. Hot Topics Evolving Medical Therapy in Interventional Cardiology: Evidence to Innovation Friday, May 1, 2:55 PM ~ 4:20 PM Presentation Theater 2, Level 1 Check the Session

May 14, 2026 49

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TCTAP 2026

Six Decades of Coronary Revascularization: CABG¡¯s Enduring Edge N

David Paul Taggart, MD, PhD (University of Oxford, United Kingdom), recipient of the 16th TCTAP Master of the Masters Award, delivered a sweeping assessment of coronary revascularization spanning the field¡¯s six-decade history-from Favaloro¡¯s first bypass graft in 1967 to the latest generation of drug-eluting stents. His verdict: despite relentless advances in percutaneous coronary intervention (PCI), coronary artery bypass grafting (CABG) retains a durable survival advantage in most patients with multivessel or left main disease, and wide geographic variation in PCI-to-CABG ratios reflects physician preference more than evidence. A Tale of Two Pioneers In 1967, René Favaloro-the ¡®father of CABG¡¯-reported the systematic use of reversed saphenous vein grafting to treat multivessel coronary artery disease. Almost a decade later, Andreas Grüntzig described the opening of stenosed coronary arteries with a balloon, laying the foundation for interventional cardiology. Despite this parallel evolution, he was unequivocal: the long-predicted demise of CABG has not occurred. The fundamental CABG operation has changed little in 60 years, with saphenous vein increasingly replaced by the internal mammary artery and other arterial conduits. In contrast, PCI has evolved through numerous stent generations. Yet even contemporary PCI, he stressed, does not match CABG outcomes in many patients with complex disease. The long-predicted demise of CABG has not occurred. Despite never-ending improvements in stent technology, PCI does not match the results of CABG in many patients with multivessel or left main disease. David Paul Taggart, MD, PhD Multivessel Disease: SYNTAX and FAME III Early trials comparing PCI and CABG were confounded by enrolling patients with low-complexity disease that poorly reflected real-world practice. The SYNTAX trial addressed this by adopting a relative ¡°all-comers¡± design-though 40% of screened patients had disease so severe they were referred directly for CABG rather than randomized. At five years, CABG demonstrated a significant overall survival advantage of approximately 5% over PCI, accompanied by marked reductions in myocardial infarction (MI) and the need for repeat revascularization. Crucially, when patients were stratified by SYNTAX score, the survival benefit of CABG widened with increasing disease complexity-roughly 7% in the intermediate-score group and 9% in the highest-risk tier. More recently, the FAME III trial, using fractional flow reserve (FFR)-guided PCI with contemporary drug-eluting stents, still failed to match CABG outcomes. These advantages are further amplified in patients with diabetes and impaired ventricular function, he noted. Trial / Comparison Key Finding CABG Advantage SYNTAX (MVD, 5-yr) All-cause mortality, MI, repeat revasc. ~5% overall survival benefit SYNTAX (High SYNTAX Score) Survival by disease severity +9% survival vs PCI FAME III (FFR-guided PCI) Contemporary DES vs CABG CABG still superior EXCEL (LMD, 5-yr) SYNTAX score ¡Â32 Clear survival benefit; ¡éMI Table: Selected landmark trials comparing CABG and PCI. MVD = multivessel disease; LMD = left main disease; DES = drug-eluting stent; MI = myocardial infarction. Left Main Disease: The EXCEL Controversy The left main (LM) coronary artery debate has proven more contentious. The EXCEL trial-the most definitive study in selected LM disease with SYNTAX scores below 32-demonstrated a clear and accelerating survival benefit for CABG at five years, along with a marked reduction in MI on conventional biochemical definitions. Yet the cardiology literature subsequently became flooded with meta-analyses combining EXCEL results with smaller, underpowered studies of less severe disease, effectively diluting the mortality signal until CABG¡¯s benefit ¡°disappeared¡± from pooled estimates. Today, there is broad consensus that LM disease with SYNTAX scores above 32 is an indication for CABG unless contraindicated. Lesser-severity LM disease remains debated. He acknowledged a notable exception: patients with true ostial or isolated mid-shaft LM stenosis may achieve excellent outcomes with PCI-possibly because competitive flow from bypass grafts reduces graft efficacy in anatomically favorable lesions. Why CABG Retains Its Edge: Three Fundamental Differences ending improvements in stent technology, and whose benefits grow ever more durable with longer follow-up-extending beyond 10 years. He emphasized the most important: 1. Bypass grafts protect the whole proximal coronary circulation-independent of the complexity of the proximal culprit lesion and from the progression of, or development of, further proximal disease. This is witnessed by the sustained reduction in subsequent myocardial infarction with CABG versus PCI in longer-term studies. 2. The internal thoracic artery exerts beneficial vasoactive effects that may actively promote long-term vessel health-a biological property no stent platform can replicate. 3. CABG more reliably achieves complete revascularization, a factor consistently associated with improved long-term outcomes across disease subsets. The PCI:CABG Ratio Gap—Evidence vs. Practice Perhaps the most provocative element of his lecture was his challenge to the global mismatch between evidence and practice. Despite more than two decades of trial data demonstrating CABG¡¯s superiority for most patients with multivessel and left main disease, the ratio of PCI to CABG varies enormously among countries and even within regions of the same country—variations that cannot be explained by differences in patient populations alone. Both PCI and CABG are complementary therapies when used in appropriate patients, he acknowledged. But he was blunt about the evidence gap: best evidence has demonstrated the superiority of CABG for most patients with multivessel and left main disease for over two decades. Given the same evidence base, the enormous discrepancies in PCI-to-CABG ratios across countries—and within regions of the same country—have only one plausible explanation: ¡°clinical practice is largely dictated by physician preference rather than evidence basis, and that may be detrimental to the best interests of the patient.¡± The Heart Team Imperative His prescription was clear: the only effective solution is properly constituted multidisciplinary heart teams empowered to make evidence-based recommendations—so that patients can then make a truly informed decision. Both procedures, he stressed, are complementary when deployed in the right patient. The gulf between evidence and practice, he implied, is a failure not of science but of how clinical decisions are made. The lecture offered a sweeping reminder that six decades of evidence consistently point in the same direction—and that the greatest remaining challenge may not be technological, but organizational. Taggart reports no relevant conflicts of interest. TCTAP Award 2026 16th TCTAP Master of the Masters Award Thursday, April 30, 11:25 AM ~ 11:55 AM Main Arena, Level 1 Check the Session

May 01, 2026 82

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TCTAP 2026

¡®Practical Guideline for Bifurcation PCI: Don't Touch!¡¯ N

At TCTAP 2026, during the ¡°Bifurcation PCI in 2026: Evolving Strategies and Key Controversies¡± session, Seung-Jung Park, MD, PhD (Asan Medical Center, Korea) will deliver a forward-looking lecture that will redefine contemporary approaches to non-left main (non-LM) bifurcation PCI in the era following the ISCHEMIA trial. His central message will be both provocative and practice-changing: ¡°Don¡¯t touch small side branches.¡± Drawing on robust evidence from randomized trials and meta-analyses, he will emphasize that percutaneous coronary intervention (PCI) will not confer a survival benefit over optimal medical therapy (OMT) in patients with stable ischemic heart disease-even among those with multivessel disease or moderate to severe ischemia. This paradigm shift will fundamentally reshape the goals of revascularization, moving from anatomical completeness toward physiologic relevance and symptom-driven intervention. A key concept that will be highlighted is the true myocardial significance of side branches. Based on fractional myocardial mass (FMM) data, the majority of side branches in non-LM bifurcation lesions will supply less than 10% of the total myocardium. In practical terms, this will mean that most side branches-particularly those with a reference vessel diameter 2.5 mm), however, a more nuanced approach will be required. In cases of true bifurcation lesions-such as Medina 1,1,1 or 0,1,1-he will advocate for upfront two-stent strategies, particularly when the side branch supplies a substantial myocardial territory or when symptoms are present. Nonetheless, even in these scenarios, treatment decisions will be guided by clinical and physiologic relevance rather than angiographic appearance alone. He will conclude by summarizing his practical clinical rules for non-LM bifurcation PCI: 1. Do not treat small side branches (

May 01, 2026 97

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TCTAP 2026

M-TEER in Secondary Mitral Regurgitation: Evidence That Shapes Practice N

At TCTAP 2026, Gregg W. Stone, MD (Mount Sinai, USA) will deliver a comprehensive lecture on mitral transcatheter edge-to-edge repair (M-TEER) in secondary mitral regurgitation (MR), synthesizing the pivotal randomized controlled trial data that has come to define contemporary clinical practice in this challenging patient population. Secondary MR, also known as functional MR (FMR), arises not from intrinsic leaflet pathology but from left ventricular remodeling and dysfunction, making its management fundamentally different from primary MR. He will begin by framing the central debate that has dominated the field: the divergent outcomes of three landmark randomized trials-COAPT, MITRA-FR, and RESHAPE-HF2-each of which enrolled patients with heart failure and FMR treated with guideline-directed medical therapy (GDMT), with or without M-TEER using the MitraClip device. Key Inclusion Criteria Across Three Major M-TEER Randomized Trials Criteria COAPT (n=614) MITRA-FR (n=304) RESHAPE-HF2 (n=505) NYHA class II-IVa II-IV II-IVa LVEF 20-50% 15-40% 20-50% LVESD 70 mmHg No exclusions No exclusions RV dysfunction Exclude moderate or severe No exclusions Exclude severe TR Exclude severe w/planned intervention No exclusions Exclude severe The COAPT trial (n=614) demonstrated a striking benefit of MitraClip added to maximally tolerated GDMT. Hospitalizations for heart failure were reduced by 47% (67.9%/yr vs. 35.8%/yr; HR 0.53 [95% CI 0.40-0.70], P=0.000006), with a number needed to treat (NNT) of just 3.1 at 24 months. All-cause mortality was similarly reduced, with 29.1% in the MitraClip group versus 46.1% in the GDMT-alone group at 24 months (HR 0.62 [95% CI 0.46-0.82], P=0.0007; NNT 5.9). Patient-reported quality of life, as assessed by the Kansas City Cardiomyopathy Questionnaire Overall Summary Score (KCCQ-OSS), showed sustained and clinically meaningful improvements of more than 12 points above the minimum clinically important difference throughout the two-year follow-up period in the device arm. In contrast, MITRA-FR (n=304) showed no benefit of MitraClip over medical therapy alone at 24 months, with nearly identical rates of death or heart failure hospitalization in both groups (63.8% vs. 67.1%; HR 1.01 [95% CI 0.77-1.34], P=0.92). He will emphasize that the divergence between COAPT and MITRA-FR was largely explained by patient selection differences. Critically, COAPT enrolled patients with "disproportionately severe" MR-defined by a high effective regurgitant orifice area (EROA) relative to left ventricular end-diastolic volume (LVEDV)-while MITRA-FR enrolled patients with relatively "proportionate" MR, where the degree of regurgitation was more commensurate with the extent of LV dilation. He will then turn to the RESHAPE-HF2 trial (n=505), which provided additional confirmatory evidence supporting M-TEER in appropriately selected patients. The trial met its co-primary endpoints, demonstrating a 36% relative risk reduction in the composite of cardiovascular death or heart failure hospitalization (rate ratio 0.64 [95% CI 0.48-0.85]; P=0.002), and a 41% reduction in heart failure hospitalizations alone (rate ratio 0.59 [95% CI 0.42-0.82]; P=0.002), with an NNT of 8.3 to prevent one death or HFH. Quality of life improvements on the KCCQ-OSS at one year were also significantly greater in the device group (mean difference 10.9 points; 95% CI 6.8-15.0; P

May 01, 2026 52

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TCTAP 2026

Angiography-Derived Physiology for PCI: The ALL-RISE Trial N

At the Late-Breaking Clinical Trials session during TCTAP 2026, William F. Fearon, MD (Stanford University School of Medicine, USA) will present the highly anticipated results of the ALL-RISE trial. Assessing coronary physiology with an intracoronary pressure wire improves clinical outcomes in patients undergoing cardiac catheterization and percutaneous coronary intervention (PCI). However, the clinical use of pressure wire-based physiology remains low. During his lecture, he will explain that the measurement of fractional flow reserve (FFR) derived from coronary angiographic images alone (FFRangio) correlates well with pressure wire-based FFR and may simplify procedures, but its effect on clinical outcomes has remained unknown. In this multicenter, international, non-inferiority trial, patients undergoing coronary angiography who were found to have at least one intermediate coronary stenosis were randomized to FFRangio or to wire-based physiologic assessment. The primary outcome was a composite of death, myocardial infarction, or unplanned clinically indicated coronary revascularization at one year, which was tested for non-inferiority with an absolute margin of 3.5%. Key secondary endpoints included procedural time, radiation exposure, and contrast media utilization. From 59 sites, 1,930 patients were randomized to either FFRangio (n=965) or to wire-based assessment (n=965). The composite endpoint of death, myocardial infarction, or revascularization occurred in 6.9% of those randomized to FFRangio and 7.1% of those randomized to wire-based assessment (difference, -0.2%; upper 97.5% CI, 2.1%), p=0.0008 for non-inferiority). Furthermore, the event rates for each component of the composite were similar between the two randomized groups. Figure 1. Kaplan-Meier Curve for the Primary Endpoint. The graph illustrates the cumulative incidence of the primary composite endpoint over 12 months since randomization. The red line represents the FFRangio group, while the blue line represents the Pressure Wire group. Beyond the primary clinical endpoints, the FFRangio-guided strategy reduced procedural time, radiation exposure, and contrast media utilization. These reductions will greatly benefit daily catheterization lab efficiency and safety. He will conclude that in patients with intermediate coronary disease requiring physiologic assessment in the cardiac catheterization laboratory, an FFRangio-guided strategy streamlined the procedure and was non-inferior with respect to clinical outcomes at one year compared with a pressure wire-guided strategy. These findings may support the broader integration of image-based physiological assessments as a viable alternative in routine PCI workflows. Clinical Science Late-Breaking Clinical Trials 2026 Friday, May 1, 8:30 AM ~ 9:55 AM Presentation Theater 1, Level 1 Check the Session

May 01, 2026 51

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TCTAP 2026

PCI vs. CABG in Diabetic Multivessel Disease: A Turning Point in the Era of Contemporary Revasculari... N

At TCTAP 2026, Duk-Woo Park, MD, PhD (Asan Medical Center, Korea), will present a timely lecture addressing one of the most enduring controversies in interventional cardiology: the optimal revascularization strategy for patients with diabetes mellitus and multivessel coronary artery disease. For decades, coronary artery bypass grafting (CABG) has been regarded as the standard of care in this high-risk population, supported by landmark randomized trials such as FREEDOM and BARI-2D. These studies demonstrated superior outcomes of CABG over percutaneous coronary intervention (PCI), particularly in reducing death and myocardial infarction. However, a critical limitation exists. These trials were conducted in an era that does not reflect contemporary clinical practice. First-generation drug-eluting stents, limited use of intravascular imaging, and absence of modern guideline-directed medical therapy-including sodium-glucose cotransporter-2 inhibitors and glucagon-like peptide-1 receptor agonists -raise concerns regarding the applicability of historical data to current patients. Over the past decade, PCI has undergone a profound transformation. Advances include next-generation drug-eluting stents, routine use of intravascular imaging (intravascular ultrasound (IVUS) and optical coherence tomography (OCT)), physiology-guided PCI using fractional flow reserve (FFR0 or instantaneous wave-free ratio (iFR), and integration of contemporary medical therapy. Modern PCI is no longer a purely device-based intervention, but rather a comprehensive, optimized strategy. In this context, the DEFINE-DM trial has been designed to address the critical evidence gap. This multicenter randomized trial will enroll approximately 1,500 patients with diabetes and three-vessel disease, comparing state-of-the-art PCI with contemporary CABG. The PCI arm will incorporate mandatory imaging and physiology guidance, while both groups will receive optimized medical therapy. The primary endpoint will be a composite of all-cause death, myocardial infarction, or stroke at 2 years, with the study powered to test non-inferiority of PCI. Importantly, DEFINE-DM represents more than a comparison of two revascularization techniques. It evaluates two fully optimized treatment strategies in the modern era. This distinction marks a paradigm shift in how revascularization trials should be interpreted. If PCI demonstrates comparable outcomes to CABG, it could significantly expand treatment options and influence future clinical guidelines. Conversely, if CABG remains superior, it will reinforce its role as the gold standard even in the contemporary era. Ultimately, the management of diabetic multivessel coronary artery disease stands at a critical crossroads. DEFINE-DM is expected to provide definitive evidence to guide the next generation of revascularization strategies and shape clinical decision-making worldwide. TCTAP Workshops Left Main & Multi-Vessel Disease: Modern Evidence and Real-World Strategy Thursday, April 30, 2:50 PM ~ 4:25 PM Main Arena, Level 1 Check the Session

April 30, 2026 67

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TCTAP 2026

TAVR Valve Durability in 2026 N

At the upcoming TCTAP 2026 conference, Tullio Palmerini, MD (S. Orsola-Malpighi Polyclinic, Italy) will present an essential clinical update on structural longevity. His presentation, focusing on transcatheter heart valve durability, will address the evolving paradigm of lifetime management. As indications for transcatheter aortic valve replacement will increasingly expand toward younger and lower-risk patients with severe aortic valve stenosis, their longer life expectancy will make valve durability a critical determinant of clinical success. The potential need for future reinterventions will dictate that the cardiovascular community will meticulously evaluate how these bioprosthetic valves will perform over the coming decades. During the session, he will elucidate that transcatheter heart valve durability will be affected by multiple physiological factors, resulting in bioprosthetic valve dysfunction. This dysfunction will be systematically classified into structural valve degeneration, non-structural valve degeneration, valve thrombosis, and infective endocarditis. The presentation will strictly adhere to the standardized Valve Academic Research Consortium-3 definitions. According to these criteria, bioprosthetic valve dysfunction will lead to bioprosthetic valve failure. The progression will be categorized into three distinct stages. Stage I will occur when the dysfunction becomes clinically manifest or when irreversible hemodynamic valve deterioration takes place. Stage II will be defined by the absolute necessity for an aortic valve reintervention. Finally, stage III will be documented in the event of a patient's death directly resulting from the bioprosthetic valve failure. A central component of the lecture will focus on structural valve degeneration, which will represent a primary mechanism of valve failure. Structural valve degeneration will involve intrinsic and structural changes within the bioprosthetic leaflets. These progressive alterations will include continuous wear and tear, leaflet disruption, flail leaflet mechanisms, fibrosis, progressive calcification, and strut fracture or deformation. These physical changes will occur in direct association with a progressive hemodynamic deterioration of the valve. He will emphasize that fully understanding the mechanistic underpinnings of structural valve degeneration will be of the utmost importance. This knowledge will be crucial for accurate patient risk stratification, the implementation of forward-looking therapeutic strategies, and the comprehensive lifetime management of younger demographics. Although clinical relevance will remain high, it will be noted that data regarding the exact predictors of structural valve degeneration will still require extensive future research. To provide concrete benchmarks, the presentation will project detailed comparative outcomes from landmark randomized controlled trials, contrasting transcatheter procedures with traditional surgical aortic valve replacement. These clinical trials will provide evidence to guide decision-making for future patients. First, the 10-year follow-up data from the NOTION trial, involving patients with a mean age of 79 years, will be reviewed. The findings will demonstrate that the incidence of severe structural valve degeneration will be significantly lower in the transcatheter group at 1.5 percent, compared to 10.0 percent in the surgical group. However, the overall rates of bioprosthetic valve failure will show no significant divergence between the two groups. Subsequently, the session will divide the 7-year follow-up results from the PARTNER III trial, which focused on a low-risk population with a mean age of 73. The projected data will indicate that the rates of Stage II and Stage III structural valve degeneration will remain comparable, at 7.3 percent for the transcatheter group and 7.6 percent for the surgical group. Furthermore, bioprosthetic valve failure rates will demonstrate parity at 6.9 percent and 7.3 percent, respectively. While valve thrombosis will be slightly higher in the transcatheter group at 2.8 percent versus 0.5 percent, these cases will largely resolve through standard anticoagulation therapies. The 5-year follow-up data from the Evolut Low Risk trial, encompassing patients with a mean age of 74, will further consolidate this landscape. Bioprosthetic valve dysfunction will be highly similar between the transcatheter group at 13.4 percent and the surgical group at 14.7 percent. Bioprosthetic valve failure will also be equivalent at 6.0 percent versus 5.6 percent. Notably, rates of patient-prosthesis mismatch and endocarditis will be lower with the transcatheter approach. A critical segment of the talk will then address a recently reported partial analysis from the 7-year follow-up of the Evolut trial. This analysis will reveal higher rates of reintervention with the transcatheter approach at 9.8 percent, compared to 6.0 percent for surgery, predominantly driven by aortic regurgitation. A post-hoc analysis will identify off-label post-dilation, specifically within the Evolut R 34mm valve, as the primary mechanical driver for this increased reintervention rate. A benchmark study will suggest that utilizing larger-than-recommended balloons will induce a spectrum of leaflet damage at the commissure level, ranging from microscopic tears to macroscopic ruptures. Despite these technical challenges, a deeply reassuring clinical observation will be emphasized. The requirement for reintervention will not be associated with an increased risk of mortality. The overall rates of death, stroke, or aortic valve-related hospitalization will remain remarkably similar between the transcatheter and surgical modalities. Concluding the session, he will firmly reiterate that transcatheter heart valve durability will be the absolute cornerstone for managing younger, lower-risk patients. Because robust data will remain limited at the mid-term mark, he will advocate that further data spanning at least a continuous 10-year follow-up will be strictly required before universally extending these transcatheter indications. Until then, the 5-year data for the Evolut-CoreValve platform and the 7-year data for the Sapien platform will confidently show that transcatheter durability will rival traditional surgery. Ultimately, this session will empower clinicians with the predictive knowledge required to optimize lifelong cardiovascular care in a rapidly advancing technological era. TCTAP Workshops Comprehensive TAVR Management Thursday, April 30, 8:30 AM ~ 10:00 AM Valve & Endovascular Theater, Level 1 Check the Session

April 30, 2026 43

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TCTAP 2026

Tailored DAPT in High-Risk Complex PCI: Still a Theory in Search of Proof N

At the scientific session, ¡°Evolving Antiplatelet Therapy After PCI: Toward Safer and Smarter Strategies,¡± taking place on April 30 in Room 202, Davide Capodanno, MD (Azienda Ospedaliero Universitaria Policlinico "G. Rodolico-San Marco", University of Catania, Italy) will address a central challenge in contemporary percutaneous coronary intervention (PCI): how to balance thrombotic protection against bleeding risk in patients undergoing complex or high-risk procedures. As PCI practice evolves, the traditional ¡°one-size-fits-all¡± approach to dual antiplatelet therapy (DAPT) will increasingly give way to more individualized strategies. A key concept to be discussed will be the temporal modulation of antiplatelet therapy. This strategy will involve early intensification of platelet inhibition to reduce peri-procedural thrombotic risk, followed by later de-escalation to minimize bleeding complications. While biologically plausible, its clinical value will remain uncertain. The lecture will focus on the TAILORED-CHIP trial, the first randomized study evaluating this time-dependent approach in complex or high-risk PCI. A total of 2,018 patients were randomized to either a tailored regimen-ticagrelor plus aspirin for six months followed by clopidogrel monotherapy-or to standard DAPT with clopidogrel and aspirin for 12 months. The primary composite endpoint of death, myocardial infarction, stroke, stent thrombosis, urgent revascularization, or clinically relevant bleeding did not significantly differ between groups (10.5% vs. 8.8%; HR 1.19; P=0.21). These findings indicate that temporal tailoring does not provide a net clinical benefit compared with standard therapy, and their implications for current clinical practice will be discussed. The lecture will further examine key limitations of the study, including lower-than-expected event rates and the heterogeneity of the study population. These factors will be discussed in terms of their impact on statistical power and the interpretation of treatment effects. The findings will be placed in the context of prior evidence, including the ALPHEUS trial, as well as current recommendations from the European Society of Cardiology. The selective use of potent P2Y12 inhibitors and the importance of individualized decision-making will be emphasized. Finally, future research directions will be outlined. These will include the need for better patient selection, optimization of treatment timing, and the potential integration of precision medicine approaches such as genetic or biomarker-guided therapy. In summary, this lecture will review current evidence and ongoing uncertainties surrounding tailored DAPT in complex PCI. While the concept of time-dependent modulation remains promising, its clinical benefit has yet to be established, and further investigation will be required before routine implementation can be recommended. Kang DY, et al. European Heart Journal, https://doi.org/10.1093/eurheartj/ehaf652 TCTAP Workshops Evolving Antiplatelet Therapy After PCI: Toward Safer and Smarter Strategies Thursday, April 30, 8:30 AM ~ 9:50 AM Room 202, Level 2 Check the Session

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Good People, Good Memories, Good Life!
Good People, Good Memories, Good Life!